Cas 4142-68-1,4,4'-((ethane-1,2-diylbis(sulfanediyl))bis(methylene))bis(2,6-di-tert-butylphenol)

4142-68-1

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Basic information

Product Name: 4,4'-((ethane-1,2-diylbis(sulfanediyl))bis(methylene))bis(2,6-di-tert-butylphenol)
Synonyms: 4,4'-((ethane-1,2-diylbis(sulfanediyl))bis(methylene))bis(2,6-di-tert-butylphenol)
CAS NO:4142-68-1
Molecular Formula:
Molecular Weight: 530.88
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4,4'-((ethane-1,2-diylbis(sulfanediyl))bis(methylene))bis(2,6-di-tert-butylphenol)(CAS DataBase Reference)
NIST Chemistry Reference: 4,4'-((ethane-1,2-diylbis(sulfanediyl))bis(methylene))bis(2,6-di-tert-butylphenol)(4142-68-1)
EPA Substance Registry System: 4,4'-((ethane-1,2-diylbis(sulfanediyl))bis(methylene))bis(2,6-di-tert-butylphenol)(4142-68-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 4142-68-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 4142-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4142-68:
(6*4)+(5*1)+(4*4)+(3*2)+(2*6)+(1*8)=71
71 % 10 = 1
So 4142-68-1 is a valid CAS Registry Number.

4142-68-1Upstream product

88-26-6 3,5-di-tert-butyl-4-hydroxybenzyl alcohol

4142-68-1Downstream Products

4142-68-1Relevant academic research and scientific papers

Design and synthesis of sulfur-containing butylated hydroxytoluene: antioxidant potency and selective anticancer agent

Ahmad, Mohd H,Rahman, Noorsaadah Abd,Kadir, Farkaad A,Al-Ani, Lina A,Hashim, Najihah M,Yehye, Wageeh A

, (2019)

Abstract: In the present study, a series of multipotent antioxidants (MPAOs), namely sulfur-containing BHT (S-BHT), derivatives were rationally designed and synthesized, and their inhibitory activities against free radicals and human cancer cell lines, HT

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